1,3,5-Trihydroxy-6-methoxy-7-(3-methylbut-2-enyl)xanthen-9-one

Details

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Internal ID dfdb2977-d813-4da8-b8a4-5aa71a1d5bc6
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 2-prenylated xanthones
IUPAC Name 1,3,5-trihydroxy-6-methoxy-7-(3-methylbut-2-enyl)xanthen-9-one
SMILES (Canonical) CC(=CCC1=CC2=C(C(=C1OC)O)OC3=CC(=CC(=C3C2=O)O)O)C
SMILES (Isomeric) CC(=CCC1=CC2=C(C(=C1OC)O)OC3=CC(=CC(=C3C2=O)O)O)C
InChI InChI=1S/C19H18O6/c1-9(2)4-5-10-6-12-16(22)15-13(21)7-11(20)8-14(15)25-19(12)17(23)18(10)24-3/h4,6-8,20-21,23H,5H2,1-3H3
InChI Key KRVKWYDGEFEJRI-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H18O6
Molecular Weight 342.30 g/mol
Exact Mass 342.11033829 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 4.30
Atomic LogP (AlogP) 3.58
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,3,5-Trihydroxy-6-methoxy-7-(3-methylbut-2-enyl)xanthen-9-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9524 95.24%
Caco-2 + 0.6429 64.29%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.4762 47.62%
OATP2B1 inhibitior - 0.5518 55.18%
OATP1B1 inhibitior + 0.8628 86.28%
OATP1B3 inhibitior + 0.9533 95.33%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.6503 65.03%
P-glycoprotein inhibitior - 0.5684 56.84%
P-glycoprotein substrate - 0.6683 66.83%
CYP3A4 substrate + 0.5648 56.48%
CYP2C9 substrate - 0.5929 59.29%
CYP2D6 substrate - 0.8145 81.45%
CYP3A4 inhibition - 0.6906 69.06%
CYP2C9 inhibition + 0.8689 86.89%
CYP2C19 inhibition + 0.9093 90.93%
CYP2D6 inhibition + 0.8517 85.17%
CYP1A2 inhibition + 0.9077 90.77%
CYP2C8 inhibition + 0.5379 53.79%
CYP inhibitory promiscuity + 0.9280 92.80%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6717 67.17%
Eye corrosion - 0.9887 98.87%
Eye irritation + 0.6264 62.64%
Skin irritation - 0.7360 73.60%
Skin corrosion - 0.9462 94.62%
Ames mutagenesis + 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5296 52.96%
Micronuclear - 0.5200 52.00%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.7965 79.65%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.7855 78.55%
Acute Oral Toxicity (c) III 0.6586 65.86%
Estrogen receptor binding + 0.8748 87.48%
Androgen receptor binding + 0.6057 60.57%
Thyroid receptor binding - 0.5843 58.43%
Glucocorticoid receptor binding + 0.8127 81.27%
Aromatase binding + 0.7738 77.38%
PPAR gamma + 0.9362 93.62%
Honey bee toxicity - 0.8150 81.50%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9832 98.32%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.63% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.72% 94.45%
CHEMBL2581 P07339 Cathepsin D 95.07% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 94.01% 94.73%
CHEMBL1929 P47989 Xanthine dehydrogenase 92.20% 96.12%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.37% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.28% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.27% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.23% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.01% 94.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.85% 93.99%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.85% 99.23%
CHEMBL1951 P21397 Monoamine oxidase A 85.79% 91.49%
CHEMBL3194 P02766 Transthyretin 85.61% 90.71%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.58% 92.62%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 81.55% 98.11%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Cratoxylum cochinchinense

Cross-Links

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PubChem 162866654
LOTUS LTS0235204
wikiData Q105145259